Dies ist eine Übersichtsseite mit Metadaten zu dieser wissenschaftlichen Arbeit. Der vollständige Artikel ist beim Verlag verfügbar.
Lung cancer prediction from microarray data by gene expression programming
59
Zitationen
4
Autoren
2016
Jahr
Abstract
Lung cancer is a leading cause of cancer-related death worldwide. The early diagnosis of cancer has demonstrated to be greatly helpful for curing the disease effectively. Microarray technology provides a promising approach of exploiting gene profiles for cancer diagnosis. In this study, the authors propose a gene expression programming (GEP)-based model to predict lung cancer from microarray data. The authors use two gene selection methods to extract the significant lung cancer related genes, and accordingly propose different GEP-based prediction models. Prediction performance evaluations and comparisons between the authors' GEP models and three representative machine learning methods, support vector machine, multi-layer perceptron and radial basis function neural network, were conducted thoroughly on real microarray lung cancer datasets. Reliability was assessed by the cross-data set validation. The experimental results show that the GEP model using fewer feature genes outperformed other models in terms of accuracy, sensitivity, specificity and area under the receiver operating characteristic curve. It is concluded that GEP model is a better solution to lung cancer prediction problems.
Ähnliche Arbeiten
Analysis of Relative Gene Expression Data Using Real-Time Quantitative PCR and the 2−ΔΔCT Method
2001 · 179.880 Zit.
Gene set enrichment analysis: A knowledge-based approach for interpreting genome-wide expression profiles
2005 · 55.981 Zit.
<tt>edgeR</tt> : a Bioconductor package for differential expression analysis of digital gene expression data
2009 · 44.088 Zit.
limma powers differential expression analyses for RNA-sequencing and microarray studies
2015 · 42.368 Zit.
clusterProfiler: an R Package for Comparing Biological Themes Among Gene Clusters
2012 · 37.531 Zit.